Canonical Allele Identifier: CA1200786094
Gene: NTRK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156876426_156876427delinsTC , CM000663.2:g.156876426_156876427delinsTC GRCh38
NC_000001.10:g.156846218_156846219delinsTC , CM000663.1:g.156846218_156846219delinsTC GRCh37
NC_000001.9:g.155112842_155112843delinsTC NCBI36
NG_007493.1:g.65677_65678delinsTC , LRG_261:g.65677_65678delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000674537.2:c.1479_1480delinsTC ENSP00000502725.1:p.Ala493=
ENST00000392302.7:c.1479_1480delinsTC ENSP00000376120.3:p.Ala493=
ENST00000497019.7:c.*251_*252delinsTC ENSP00000436804.2:n.*251_*252delinsTC
ENST00000524377.7:c.1659_1660delinsTC MANE Select ENSP00000431418.1:p.Ala553=
ENST00000674537.1:c.1479_1480delinsTC ENSP00000502725.1:p.Ala493=
ENST00000358660.3:c.1650_1651delinsTC ENSP00000351486.3:p.Ala550=
ENST00000368196.7:c.1641_1642delinsTC ENSP00000357179.3:p.Ala547=
ENST00000392302.6:c.1551_1552delinsTC ENSP00000376120.2:p.Ala517=
ENST00000497019.6:c.*251_*252delinsTC ENSP00000436804.1:n.*251_*252delinsTC
ENST00000524377.5:c.1659_1660delinsTC ENSP00000431418.1:p.Ala553=
ENST00000530298.5:n.2112_2113delinsTC
NM_001007792.1:c.1551_1552delinsTC , LRG_261t1:c.1551_1552delinsTC NP_001007793.1:p.Ala517=
NM_001012331.1:c.1641_1642delinsTC , LRG_261t2:c.1641_1642delinsTC NP_001012331.1:p.Ala547=
NM_002529.3:c.1659_1660delinsTC , LRG_261t3:c.1659_1660delinsTC NP_002520.2:p.Ala553=
NM_001012331.2:c.1641_1642delinsTC NP_001012331.1:p.Ala547=
NM_002529.4:c.1659_1660delinsTC MANE Select NP_002520.2:p.Ala553=